Reaktion #44955

ord-21d687e9fc524443be04ee0bd85f33bb

Reaktionsgleichung

[Ca+2].[Cl-].[Cl-]
calcium chloride
[K+].[OH-]
potassium hydroxide
C/C(=C\C(=O)OCCCCCCCCC(=O)O)C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O
pseudomonic acid
[K+].[OH-]
potassium hydroxide
[K+].[OH-]
potassium hydroxide
[Ca+2].[Cl-].[Cl-]
calcium chloride
[Ca+2].[Cl-].[Cl-]
calcium chloride
C/C(=C\C(=O)OCCCCCCCCC(=O)O)C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O.[K]
mupirocin potassium
C/C(=C\C(=O)OCCCCCCCCC(=O)O)C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O
Pseudomonic acid
C/C(=C\C(=O)OCCCCCCCCC(=O)[O-])C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O.C/C(=C\C(=O)OCCCCCCCCC(=O)[O-])C[C@@H]1OC[C@H](C[C@@H]2O[C@H]2[C@@H](C)[C@H](C)O)[C@@H](O)[C@H]1O.[Ca+2]
Mupirocin Calcium

Reaktionsbedingungen

Temperatur
24.5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigekept at 25-27° C
  2. 2
    Sonstigeuntil obtaining
  3. 3
    FiltrationPotassium chloride was filtered
  4. 4
    workup.ADDITIONSolution B (25 ml) was added to diisopropyl-ether (250 ml) at (−7)° C
  5. 5
    workup.STIRRINGwhile stirring
  6. 6
    SonstigeSolid amorphous mupirocin calcium precipitated from the solution
  7. 7
    workup.STIRRINGwas stirred at −7° C. for 3 h
  8. 8
    FiltrationThe solid product was filtered
  9. 9
    Waschenwashed with cold diisoprpyl-ether (10 ml)
  10. 10
    SonstigeThe product was dried in a fluidized bed dryer for 6 hours at 35° C.
  11. 11
    Sonstigefor 12 h
  12. 12
    Sonstigeat 35° C.

Vorschrift

Pseudomonic acid (220 g) was dissolved in methanol (210 ml) kept at 25-27° C. Separately, potassium hydroxide (27.9 g) was dissolved in methanol (154 ml). Also separately, calcium chloride (24.39 g) was dissolved in methanol (133 ml). The potassium hydroxide solution was added to the pseudomonic acid solution until obtaining a pH=9.4-9.5 (147 ml of potassium hydroxide solution was added.). The calcium chloride solution was then added to the mupirocin potassium solution until reaching a pH=7.6-7.7 (128 ml of calcium chloride solution was added.). The solution was stirred at 24-25° C. for an hour. Potassium chloride was filtered, and the solution was labeled Solution B. Solution B (25 ml) was added to diisopropyl-ether (250 ml) at (−7)° C. while stirring. Solid amorphous mupirocin calcium precipitated from the solution, and was stirred at −7° C. for 3 h. The solid product was filtered and washed with cold diisoprpyl-ether (10 ml). The product was dried in a fluidized bed dryer for 6 hours at 35° C., and then in a vacuum oven for 12 h at 35° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737177B2uspto-grants-2010_06